Multibranching watermelon plant and method of producing

ABSTRACT

The present invention relates to a watermelon plant, seed, variety and hybrid. More specifically, the invention relates to a watermelon plant having an allele which results in a multibranching compact watermelon plant with small fruit. The invention also relates to crossing inbreds, varieties and hybrids containing the allele to produce novel types and varieties of watermelon plants.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. §119 from U.S.application Ser. No. 10/999,650, filed Nov. 30, 2004, which isincorporated herein in its entirety by reference.

FIELD OF THE INVENTION

The present invention relates to an allele of watermelon designated“HMBN”, which results in multibranching compact plants and small fruit.The present invention also relates to a watermelon seed, a watermelonplant and parts of a watermelon plant, a watermelon variety and awatermelon hybrid which comprise the mutant allele. In addition, thepresent invention is directed to transferring the HMBN allele in thewatermelon plant to other watermelon varieties and species and is usefulfor producing new types and varieties of multibranching watermelon.

BACKGROUND OF THE INVENTION

The present invention relates to a new and distinctive watermelon mutantallele, designated “HMBN”. There are numerous steps in the developmentof any novel, desirable plant germplasm. Plant breeding begins with theanalysis and definition of problems and weaknesses of the currentgermplasm, the establishment of program goals, and the definition ofspecific breeding objectives. The next step is selection of germplasmthat possess the traits to meet the program goals. The goal is tocombine in a single variety or hybrid an improved combination ofdesirable traits from the parental germplasm. These important traits mayinclude higher yield, field performance, fruit and agronomic qualitysuch as firmness, color, content in soluble solids, acidity andviscosity, resistance to diseases and insects, and tolerance to droughtand heat.

All cultivated forms of watermelon belong to the polymorphic speciesCitrullus lanatus that is grown for its edible fruit that weigh fromfive to forty pounds, depending on variety. As a crop, watermelons aregrown commercially wherever environmental conditions permit theproduction of an economically viable yield. In the United States, themain watermelon production areas are Florida, Georgia, Texas andCalifornia. Fresh watermelon are eaten sliced or diced and may also beused as an ingredient in prepared foods.

Watermelon is thought to have originated in southern Africa because itis found growing wild throughout the area, and reaches maximum diversityof forms there. It has been cultivated in Africa for over 4,000 years.Citrullus colocynthis is considered to be a wild ancestor of watermelon.It has fruit that are small, with a maximum diameter of 75 mm, withbitter flesh and small, brown seeds. Although Citrullus species growwild in southern and central Africa, C. colocynthis also grows wild inIndia. Cultivation of watermelon began in ancient Egypt and India and isthough to have spread from those countries through the Mediterranean,Near East, and Asia. The crop has been grown in the Untied States since1629.

Citrullus lanatus is a member of the family Cucurbitaceae which consistsof about 90 genera and 700 to 760 species, mostly of the tropics. Thefamily includes pumpkins, squashes, gourds, watermelon, loofah, andseveral weeds. There are four recognized Citrullus species, C. lanatus,C. colocynthis, C. rehmii and C. ecirrhosus; all have 22 chromosomes andcan be crossed with each other successfully.

C. lanatus is an annual watermelon. It has large, broad green leaves,which are orbicular to triangular-ovate in shape and deeply three tofive lobed or sometimes simple. Medium-sized flowers are monoecious andhave short pedicels. Fruits are of medium to large size, with thick rindand solid flesh with high water content. Flesh color may be red, yellow,or white. Seeds are ovate to oblong, are strongly compressed and havewhite or brown seed coats. The root system of the plant is a deep,spreading fibrous semi-taproot system that extends six feet or morebelow the soil surface.

C. colocynthis is a perennial watermelon. It differs from C. lanatusprimarily in the size of plant organs. Leaves are small with narrowlobes, and are hairy and grayish in color. Flowers are monoecious andsmall. Bloom is profuse in autumn, when fresh vegetative growth alsooccurs. Seeds are small and brown. Fruits are small, not exceeding 3inches in diameter, with rind and spongy flesh that are always bitter.

C. ecirrhosus is a perennial watermelon. C. ecirrhosus closely resemblesC. colocynthis in vegetative characteristics, but its leaves are moredivided, are covered with dense fine hairs, and have strongly recurvedmargins. Tendrils are lacking. Fruits are subglobose with white fleshand are bitter like C. colocynthis. Flowers are not produced until thesecond year of growth.

Commercial watermelon plants are monoecious, producing both male andfemale flowers. A female flower can be easily recognized by the swellingof its base that resembles a tiny watermelon. Honeybees, mainly in themorning, pollinate the flowers. There are many diverse cultivars forproduction with varieties having dark green to yellow rind coloring,striped or solid coloring, and containing seeds or are seedless. Theshape of the fruit varies from round to elliptical.

Watermelon varieties fall into three broad classes based on how the seedwas developed: open-pollinated, F₁ hybrid and triploid (commonlyreferred to as seedless). Open-pollinated varieties are developedthrough several generations of selection. The selection can be basedupon yield, quality characteristics and disease resistance. F₁ hybridsare developed from two inbred lines that have been selfed for severalgenerations and then crossed. F₁ hybrid seed exhibit increaseduniformity of type and time of harvest compared with open-pollinatedseed and can exhibit as much as a 20 percent to 40 percent increase inyields over open-pollinated varieties grown under similar conditions.The third type is triploid or seedless watermelon. These are developedby creating watermelon plants with double the usual chromosome numberand crossing them with normal watermelon plants. The resulting plantshave one-and-a-half times the normal chromosome number. Because theyhave an odd number of chromosomes, they cannot form viable seed.Although triploid watermelons are referred to as seedless, they are nottruly seedless but rather have undeveloped seeds that are soft andedible.

Choice of breeding or selection methods depends on the mode of plantreproduction, the heritability of the trait(s) being improved, and thetype of cultivar used commercially (e.g., F₁ hybrid cultivar, purelinecultivar, etc.). For highly heritable traits, a choice of superiorindividual plants evaluated at a single location will be effective,whereas for traits with low heritability, selection should be based onmean values obtained from replicated evaluations of families of relatedplants. Popular selection methods commonly include pedigree selection,modified pedigree selection, mass selection, and recurrent selection.

The complexity of inheritance influences choice of the breeding method.Backcross breeding is used to transfer one or a few favorable genes fora highly heritable trait into a desirable cultivar. This approach hasbeen used extensively for breeding disease-resistant cultivars. Variousrecurrent selection techniques are used to improve quantitativelyinherited traits controlled by numerous genes. The use of recurrentselection in self-pollinating crops depends on the ease of pollination,the frequency of successful hybrids from each pollination, and thenumber of hybrid offspring from each successful cross.

Each breeding program should include a periodic, objective evaluation ofthe efficiency of the breeding procedure. Evaluation criteria varydepending on the goal and objectives, but should include gain fromselection per year based on comparisons to an appropriate standard,overall value of the advanced breeding lines, and number of successfulcultivars produced per unit of input (e.g., per year, per dollarexpended, etc.).

Promising advanced breeding lines are thoroughly tested and compared toappropriate standards in environments representative of the commercialtarget area(s) for three years at least. The best lines are candidatesfor new commercial cultivars; those still deficient in a few traits areused as parents to produce new populations for further selection.

These processes, which lead to the final step of marketing anddistribution, usually take from eight to 12 years from the time thefirst cross is made. Therefore, development of new cultivars is atime-consuming process that requires precise forward planning, efficientuse of resources, and a minimum of changes in direction.

A most difficult task is the identification of individuals that aregenetically superior, because for most traits the true genotypic valueis masked by other confounding plant traits or environmental factors.One method of identifying a superior plant is to observe its performancerelative to other experimental plants and to a widely grown standardcultivar. If a single observation is inconclusive, replicatedobservations provide a better estimate of its genetic worth.

The goal of watermelon plant breeding is to develop new, unique andsuperior watermelon inbreds and hybrids. The breeder initially selectsand crosses two or more parental lines, followed by repeated selfing andselection, producing many new genetic combinations. The breeder cantheoretically generate billions of different genetic combinations viacrossing, selfing and mutations. The breeder has no direct control atthe cellular level. Therefore, two breeders will never develop the sameline, or even very similar lines, having the same watermelon traits.

Each year, the plant breeder selects the germplasm to advance to thenext generation. This germplasm is grown under unique and differentgeographical, climatic and soil conditions, and further selections arethen made, during and at the end of the growing season. The varietieswhich are developed are unpredictable. This unpredictability is becausethe breeder's selection occurs in unique environments, with no controlat the DNA level (using conventional breeding procedures), and withmillions of different possible genetic combinations being generated. Abreeder of ordinary skill in the art cannot predict the final resultinglines he develops, except possibly in a very gross and general fashion.The same breeder cannot produce the same line twice by using the exactsame original parents and the same selection techniques. Thisunpredictability results in the expenditure of large research monies todevelop superior new watermelon varieties.

The development of commercial watermelon hybrids requires thedevelopment of homozygous inbred lines, the crossing of these lines, andthe evaluation of the crosses. Pedigree, backcross or recurrentselection breeding methods are used to develop lines from breedingpopulations. Breeding programs combine desirable traits from two or morelines or various broad-based sources into breeding pools from whichmutant alleles are developed by selfing and selection of desiredphenotypes. The new inbreds are crossed with other inbred lines and thehybrids from these crosses are evaluated to determine which havecommercial potential.

Pedigree breeding is used commonly for the improvement ofself-pollinating crops or inbred parents of cross-pollinating crops. Twoparents which possess favorable, complementary traits are crossed toproduce an F₁. An F₂ population is produced by selfing one or severalF₁'s or by intercrossing two F₁'s (sib mating). Selection of the bestindividuals is usually begun in the F₂ population; then, beginning inthe F₃, the best individuals in the best families are selected.Replicated testing of families, or hybrid combinations involvingindividuals of these families, often follows in the F₄ generation toimprove the effectiveness of selection for traits with low heritability.At an advanced stage of inbreeding (i.e., F₆ and F₇), the best lines ormixtures of phenotypically similar lines are tested for potentialrelease as new cultivars or new parents for hybrids.

Mass and recurrent selections can be used to improve populations ofeither self- or cross-pollinating crops. A genetically variablepopulation of heterozygous individuals is either identified or createdby intercrossing several different parents. The best plants are selectedbased on individual superiority, outstanding progeny, or excellentcombining ability. The selected plants are intercrossed to produce a newpopulation in which further cycles of selection are continued.

Backcross breeding has been used to transfer genes for a simplyinherited, highly heritable trait into a desirable homozygous cultivaror inbred which is the recurrent parent. The source of the trait to betransferred is called the donor parent. The resulting plant is expectedto have the attributes of the recurrent parent (e.g., cultivar) and thedesirable trait transferred from the donor parent. After the initialcross, individuals possessing the phenotype of the donor parent areselected and repeatedly crossed (backcrossed) to the recurrent parent.The resulting plant is expected to have the attributes of the recurrentparent (e.g., cultivar) and the desirable trait transferred from thedonor parent.

Mutation breeding is another method of introducing new traits intowatermelon varieties. Mutations that occur spontaneously or areartificially induced can be useful sources of variability for a plantbreeder. The goal of artificial mutagenesis is to increase the rate ofmutation for a desired characteristic. Mutation rates can be increasedby many different means including temperature, long-term seed storage,tissue culture conditions, radiation (such as X-rays, Gamma rays,neutrons, Beta radiation, or ultraviolet radiation), chemical mutagens(such as base analogues like 5-bromo-uracil), antibiotics, alkylatingagents (such as sulfur mustards, nitrogen mustards, epoxides,ethyleneamines, sulfates, sulfonates, sulfones, or lactones), azide,hydroxylamine, nitrous acid or acridines. Once a desired trait isobserved through mutagenesis the trait may then be incorporated intoexisting germplasm by traditional breeding techniques. Details ofmutation breeding can be found in “Principles of Cultivar Development”by Fehr, Macmillan Publishing Company, 1993.

Mutation breeding includes chromosome doubling agents such as thechemical colchicine, which inhibits microtubule formation during celldivision. When treated with colchicine, a cell's chromosomes are copiedin preparation for mitosis as normal, but the lack of microtubulesprevents cell cleavage. The result is an undivided cell that containsdouble the normal complement of the organism's chromosomes. Thecolchicine-treated cell is then regenerated into a full plant in whicheach cell has its chromosomes doubled. If an individual with mismatchedchromosomes is treated with colchicine, its chromosomes will be doubled,thus creating a matching partner chromosome that is able to match upproperly during sexual reproduction. The procedure can restore fertilityto a formerly sterile individual and the newly fertile, amphidiploidplant can then produce segregating offspring that can be observed forfurther traits. Colchicine may also be used to double the chromosomenumber of a normal, cultivated plant so that the plant may be able toreadily combine with another plant that has a different number ofchromosomes.

Descriptions of other breeding methods that are commonly used fordifferent traits and crops can be found in one of several referencebooks (e.g., Principles of Plant Breeding, John Wiley and Son, pp.115-161, 1960; Allard, 1960; Simmonds, 1979; Sneep et al., 1979; Fehr,1987).

Proper testing should detect any major faults and establish the level ofsuperiority or improvement over current cultivars. In addition toshowing superior performance, there must be a demand for a new cultivarthat is compatible with industry standards or which creates a newmarket. The introduction of a new cultivar will incur additional coststo the seed producer, the grower, processor and consumer; for specialadvertising and marketing, altered seed and commercial productionpractices, and new product utilization. The testing preceding release ofa new cultivar should take into consideration research and developmentcosts as well as technical superiority of the final cultivar. Forseed-propagated cultivars, it must be feasible to produce seed easilyand economically.

Once the inbreds that give the best hybrid performance have beenidentified, the hybrid seed can be reproduced indefinitely as long asthe homogeneity of the inbred parent is maintained. A single-crosshybrid is produced when two inbreds are crossed to produce the F₁progeny.

Watermelon has been improved by domestication and formal plant breedingfrom a late maturing vine with small fruit having hard, white flesh andbland or bitter taste, into an early maturing, more compact plant withlarge fruit having edible, sweet flesh. In the last century, plantbreeders working in public or private programs in the United States andaround the world have released varieties having disease resistance,dwarf vines, larger fruit, higher sugar content, higher lycopenecontent, seedlessness, and new flesh colors, such as dark red, orangeand yellow. Recent advances in the breeding of seedless triploid hybridshave resulted in renewed popularity of watermelons, and per capitaconsumption has increased 37% since 1980.

However, even with such a tremendous diversity, most watermelon plantsare large and produce large fruits weighing from five to forty poundswhile there is an increasing demand for smaller plants and fruits. Somesmaller plants have been discovered and a gene, dw-1, resulting in adwarf plant habit has been identified as a single recessive gene (Mohr,H. C., Proc. Assoc. Southern Agric. Work., 53:174 (1956)). Anothersingle recessive dwarfing gene, dw-2, which controls multibranching fromthe crown of the plant was identified in 1975 (Mohr, H. C. and M. S.Sandhu, J. Am. Soc. Hortic. Sci. 100:135-137).

These dwarfing genes apply only to the plant and not to the fruitresulting in large fruit on small plants. It has been very difficult forwatermelon breeders to develop small plants with small fruit andcommercially acceptable yield. Unexpectedly, the HMBN allele of thepresent invention results in both small plants and smaller fruits withcommercially acceptable yield.

SUMMARY OF THE INVENTION

The present invention provides a new allele derived from Citrulluslanatus that is phenotypically expressed by the formation of compactplants and smaller fruits when present in the homozygous state. Thismutant allele has been determined to be a single, recessive gene. Theinvention further provides plants, seeds, fruits and other plant partssuch as pollen and ovules containing the mutant allele.

The invention also provides methods for introducing the allele intoplants by crossing a variety which lacks the mutant allele with avariety that has the allele, backcrossing the progeny with the varietywhich lacks the mutant allele, selfing the resulting generations andthen selecting the plants exhibiting a compact plant and smaller fruit.

In another aspect, the invention provides a method for producing ahybrid Citrullus lanatus seed comprising crossing a first cultivar plantparent with a second cultivar plant parent and harvesting the resultanthybrid Citrullus lanatus seed, wherein both parents are cultivarscontaining the mutant allele. The hybrid seeds, plant and parts thereofproduced by such method are also part of the invention.

Another aspect of the invention relates to any watermelon seed or planthaving the mutant allele HMBN.

In another aspect, the present invention provides regenerable cells foruse in tissue culture. The tissue culture will preferably be capable ofregenerating plants having the physiological and morphologicalcharacteristics of the foregoing inbred watermelon plant, and ofregenerating plants having substantially the same genotype as theforegoing inbred watermelon plant. Preferably, the regenerable cells insuch tissue cultures will be embryos, protoplasts, meristematic cells,callus, pollen, leaves, anthers, stems, petioles, roots, root tips,fruits, seeds, flowers, cotyledons, hypocotyls or the like. Stillfurther, the present invention provides watermelon plants regeneratedfrom the tissue cultures of the invention.

DEFINITIONS

In the description and tables which follow, a number of terms are used.In order to provide a clear and consistent understanding of thespecification and claims, including the scope to be given such terms,the following definitions are provided:

Allele. “Allele” is any of one or more alternative forms of a gene, allof which alleles relate to one trait or characteristic. In a diploidcell or organism, the two alleles of a given gene occupy correspondingloci on a pair of homologous chromosomes.

Backcrossing. Backcrossing is a process in which a breeder repeatedlycrosses hybrid progeny back to one of the parents, for example, a firstgeneration hybrid F₁ with one of the parental genotypes of the F₁hybrid.

Average fruit length. “Average fruit length” means the average length incentimeters of all fruits harvested from one or more watermelon plantsof a specific genotype.

Average fruit number. “Average fruit number” means the average number offruit harvested from one or more watermelon plants of a specificgenotype.

Average fruit weight. “Average fruit weight” means the average weight inkilograms of all fruits from one or more watermelon plants of a specificgenotype.

Average fruit width. “Average fruit width” means the average width incentimeters of all fruits harvested from one or more watermelon plantsof a specific genotype.

Average internode length. “Average internode length” means the averagelength of the internodes of a watermelon plant of a specific genotypemeasured in centimeters.

Average leaf length. “Average leaf length” means the average distance ofthe leaf along the midrib from the tip to the start of the petiole.

Average leaf width. “Average leaf width” means the average distance ofthe widest part of the leaf perpendicular to the midrib of the leaf.

Average length to width ratio (L/W Ratio). “Average length to widthratio” (L/W ratio) means the average length to width ratio from allfruits harvested from one or more watermelon plants of a specificgenotype.

Average length of longest branch. “Average length of longest branch”means the average length of the longest branch of the watermelon plantin centimeters as measured from the crown of the plant.

Average length of shortest branch. “Average length of shortest branch”means the average length of the shortest branch of the watermelon plantin centimeters as measured from the crown of the plant.

Average number of female flowers. “Average number of female flowers”means the average number of pistillate flowers open per plant on aspecific day. The number of days refers to the number of days sincefirst flower.

Average number of male flowers. “Average number of male flowers” meansthe average number of staminate flowers open per plant on a specificday. The number of days refers to the number of days since first flower.

Average number of secondary branches at 30 cm. “Average number ofsecondary branches at 30 cm” means the average number of secondarybranches measured at 30 centimeters from the crown of the watermelonplant of a specific genotype.

Average number of secondary branches at 90 cm. “Average number ofsecondary branches at 90 cm” means the average number of secondarybranches measured at 90 centimeters from the crown of the watermelonplant of a specific genotype.

Chromosome doubling agent. Any one of a number of mitotic inhibitors,including colchicine, oryzalin, trifluralin, amiprophos-methyl, and N₂Ogas.

Colchicine. Colchicine is an alkaloid prepared from the corms and seedsof Colchicum autumnale, the autumn crocus. Normally after a cell hascopied its chromosomes in preparation for cell division, the spindleforms, attaches to the chromosomes and moves the chromosomes to oppositesides of the cell. The cell then divides with a set of chromosomes ineach of the daughter cells. Colchicine suppresses cell division byinhibiting formation of the spindle microtubules which prevents the cellfrom distributing the two copies of the chromosomes to opposite sides ofthe cell. The cell then fails to divide.

Diploid. Having two sets or a pair of chromosomes.

Diploid plants. “Diploid plants” means plants or transplants derivedfrom planting diploid seeds or from micro propagation.

Essentially all the physiological and morphological characteristics. Aplant having “essentially all the physiological and morphologicalcharacteristics” means a plant having the physiological andmorphological characteristics, except for the characteristics derivedfrom the converted gene.

Explosive rind. “Explosive rind” in watermelon is a trait where the rindis tender and can burst open when cut with a knife. It is caused by agene called “e”. The rind can also explode before the watermelon fruitreaches physiological maturity and results in unmarketable fruit.

Female flowers. “Female flowers” means the pistillate imperfect flowers.

Fruit firmness. “Fruit firmness” means the pressure needed in pounds topuncture the external skin of the fruit using a Fruit Pressure Tester(model FT327 with a 8.0 mm tip from the International Ripening Company,Norfolk, Virginia).

Haploid. Having the same number of sets of chromosomes as a germ cell orhalf as many as a somatic cell.

Hollowheart. “Hollowheart” is the characteristic of separation of tissuewithin the endocarp which can be caused by rapid fruit growth and weaktissue. The presence of Hollowheart (or one variant which is placentaldetachment) is affected by environment, but can also be selected againstin the development of inbred lines. The genetic control of thisundesirable trait is not understood.

Lobed leaf. “Lobed leaf” means a leaf having two or more lobes.

Male flowers. “Male flowers” means the staminate imperfect flowers.

Nonlobed leaf. “Nonlobed leaf” means a leaf that is not lobed.

Plant. “Plant” includes plant cells, plant protoplasts, plant cells oftissue culture from which watermelon plants can be regenerated, plantcalli, plant clumps and plant cells that are intact in plants or partsof plants such as pollen, flowers, seed, leaves, stems, rind, flesh andthe like.

Plant diameter. “Plant diameter” means the average length of plantmeasurements in inches.

Ploidy. The number of single sets of chromosomes in a cell or organism.

Quantitative Trait Loci (QTL). “Quantitative trait loci (QTL)” refer togenetic loci that control to some degree numerically representabletraits that are usually continuously distributed.

Regeneration. “Regeneration” refers to the development of a plant fromtissue culture.

Rind Pattern. The “rind pattern” is the coloration of the rind inwatermelons which can vary from light green, often termed gray, tomedium green to very dark green which appears to be almost black. Inaddition, the rind may have stripes of various designs which are typicalof a variety or type. Therefore the terms ‘tiger stripe’, ‘mottlestripe’, ‘dark mottle stripe’, etc. are used to identify variouspatterns.

Secondary branches. “Secondary branches” means the branches resultingfrom the splitting of the primary (crown) branches.

Seedless. “Seedless” means a watermelon fruit in which the embryodevelopment is aborted and the seed development process has stoppedbefore producing a mature viable seed. Seedless fruit may contain tracesof the developing seed and occasionally a seed coat may form and becomehard and have the appearance of a seed.

Single gene converted (conversion). “Single gene converted” (orconversion) plant refers to plants which are developed by a plantbreeding technique called backcrossing or via genetic engineeringwherein essentially all of the desired morphological and physiologicalcharacteristics of an inbred are recovered in addition to the singlegene transferred into the inbred via the backcrossing technique or viagenetic engineering.

Tetraploid. Having four times the haploid number of chromosomes in thecell nucleus.

Thick rind. “Thick rind” is inherited in a polygenic fashion (controlledby more than one gene). Thick rind is proportional with the overallfruit diameter (fruit size). A rind thickness of ¾″ is acceptable for a16 pound watermelon; but for a 10 pound watermelon the rind should be ofno more than ¼″ to be marketable.

Triploid plants. “Triploid plants” means plants or transplants derivedfrom planting triploid seeds or from micro propagation.

Vine length. “Vine length” is the length of the runners (vines) and ismeasured in inches.

Yield. “Yield” means the total weight in pounds of all watermelon fruitharvested per acre.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to a new allele designated “HMBN” in thegenus Citrullus that is phenotypically expressed in a multibranchingcompact plant and small fruit. The present invention also relates to awatermelon seed, a watermelon plant and plant parts, a watermelonvariety and a watermelon hybrid which comprise the new HMBN allele. Thepresent invention also relates to a method of producing the disclosedwatermelon plants and seeds.

The plant habit of a watermelon having the mutant allele has anoticeable increase in secondary branching compared to normal diploidsand to homozygous lines containing the dw-2 or the dw-1 genes.

The allele of the present invention is readily transferred between thedeposited cultivar and its related cultivars. The allele and the methodsof the present invention can be used to modify and reduce the weight offruits and the plant habit of all C. lanatus cultivars for commercialproduction. Generally, the methods involve emasculation of one parent,followed by application of pollen from the other parent to the stigma ofthe first parent. The crosses can be performed using either parent asthe pollen parent.

A plant of the present invention can be obtained by crossing a planthomozygous for the claimed mutant allele with any watermelon cultivarlacking the allele. The plant containing the allele can be any C.lanatus variety including a cultivar in which the factor has beenpreviously genetically fixed.

Because the HMBN allele acts as a single recessive allele, the F₁generation will not be multibranching. Only a plant homozygous for theallele will fully exhibit the multibranching phenotype. This phenotypecan be used to identify progeny that are homozygous for the claimedmutant allele. After selfing the F₁ population, the F₂ generation willexhibit the phenotype in a ratio of approximately 1:3. Backcrossing F₂multibranched individuals with a recurrent normal parent plant willproduce the backcrossed F₁ population. Selfing the backcrossed F₁population will give the backcrossed F₂ generation. As in the F₂population, the multibranching trait will segregate in a ratio of about1:3 in this population. Repeated backcrosses will produce amultibranching cultivar with the characteristics of the recurrent parentcultivar. The HMBN allele will thus become genetically fixed in theresulting cultivar. The trait may then be transmitted by sexual crossingto other cultivars if desired.

Other breeding schemes can be used to introduce the HMBN allele into thedesired cultivar. The particular scheme used is not critical to theinvention, so long as the allele is stably incorporated into the genomeof the cultivar. For example, a marker gene can be used. A nucleic acidprobe which hybridizes to the marker gene can be used to identify thedesired plants in the F₁ generation.

In order to determine if an unknown multibranching cultivar possessesthe claimed HMBN allele, a classic genetic test for allelism can beperformed. The cultivar is crossed with a plant known to possess theclaimed allele. By analyzing the resulting F₁ generation, the genotypeof the unknown cultivar can be determined. If the unknown cultivarpossesses the HMBN allele, the multibranching phenotype will be observedin the F₁ generation.

The HMBN allele is readily transferred from one cultivar to another. Thehomozygous condition is fairly easy to identify. The homozygote can beidentified early, well before flowering.

The HMBN allele will advantageously be introduced into varieties thatcontain other desirable genetic traits such as resistance to disease,early fruit maturation, drought tolerance, fruit shape, seedlessness,and the like.

The watermelon of the present invention was an unexpected mutant allelethat arose from a watermelon breeding project. A watermelon breedingline, known as line 610f5, was used in the breeding project andcontained the HMBN allele.

The watermelon mutant of the present invention was crossed into otherseed lines and into vegetative lines. A series of watermelon plantsexpressing the mutant trait in the F₂ generation was produced. Self seedfrom this series of plants yielded plants which were all multibranching.

The invention also relates to methods for producing a watermelon plantcontaining in its genetic material one or more transgenes and to thetransgenic watermelon plant produced by that method.

In another aspect, the present invention provides for single geneconverted plants of HMBN. The single transferred gene may preferably bea dominant or recessive allele. Preferably, the single transferred genewill confer a trait such as male sterility, herbicide resistance, insectresistance, resistance for bacterial, fungal, or viral disease, malefertility, early maturity, enhanced nutritional quality, and enhancedflavor. The single gene may be a naturally occurring watermelon gene ora transgene introduced through genetic engineering techniques.

The invention further provides methods for developing watermelon plantsin a watermelon plant breeding program using plant breeding techniquesincluding recurrent selection, backcrossing, pedigree breeding,restriction fragment length polymorphism enhanced selection, geneticmarker enhanced selection and transformation. Seeds, watermelon plants,and parts thereof produced by such breeding methods are also part of theinvention.

The present invention has an average fruit number of greater than 3.0,including a fruit number in the range of whole integers and partsthereof, including 3.0, 4.0, 5.0, 6.0, 7.0, 8.0, 9.0, and 10.0.

Another aspect of the present invention has an average number ofsecondary branches at 30 cm greater than 20.0, including a number ofsecondary branches at 30 cm greater than 20.0 in the range of wholeintegers and parts thereof, including 20.0, 21.0, 22.0, 23.0, 24.0,25.0, 26.0, 27.0, 28.0, 29.0, 30.0, 31.0, 32.0, 33.0, 34.0, 35.0, 36.0,37.0, 38.0, 39.0, 40.0, 41.0, 42.0, 43.0, 44.0, 45.0, 46.0, 47.0, and48.0.

Another aspect of the present invention has an average number ofsecondary branches at 90 cm greater than 19.0, including a number ofsecondary branches at 90 cm greater than 19.0 in the range of wholeintegers and parts thereof, including 19.0, 20.0, 21.0, 22.0, 23.0,24.0, 25.0, 26.0, 27.0, 28.0, 29.0, 30.0, 31.0, 32.0, 33.0, 34.0, 35.0,36.0, 37.0, 38.0, 39.0, 40.0, 41.0, 42.0, 43.0, 44.0, 45.0, 46.0, 47.0,48.0, 49.0, and 50.0.

Another aspect of the present invention has an average fruit weight ofless than 1.5 kilograms, including a fruit weight in the range of wholeintegers and parts thereof, including 1.5, 1.4, 1.3, 1.2, 1.1, 1.0, 0.9,0.8, 0.7, 0.6, 0.5, 0.4, and 0.3 kilograms.

Another aspect of the present invention has an average fruit firmness ofless than 17.0 pounds, including fruit firmness in the range of wholeintegers and parts thereof, including 17.0, 16.0, 15.0, 14.0, 13.0,12.0, 11.0, 10.0, 9.0, 8.0, 7.0, 6.0, 5.0, and 4.0 pounds.

Another aspect of the present invention has an average number of maleflowers of greater than 13.0 at day 8, including an average number ofmale flowers at day 8 in the range of whole integers and parts thereof,including 13.0, 14.0, 15.0, 16.0, 17.0, 18.0, 19.0, 20.0, 21.0, 22.0,23.0, 24.0, 25.0, 26.0, 27.0, 28.0, 29.0, 30.0, 31.0, 32.0, 33.0, 34.0,35.0, 36.0, 37.0, 38.0, 39.0, and 40.0.

Another aspect of the present invention has an average number of maleflowers of greater than 11.0 at day 15, including an average number ofmale flowers at day 15 in the range of whole integers and parts thereof,including 11.0, 12.0, 13.0, 14.0, 15.0, 16.0, 17.0, 18.0, 19.0, 20.0,21.0, 22.0, 23.0, 24.0, 25.0, 26.0, 27.0, 28.0, 29.0, and 30.0.

Another aspect of the present invention has an average number of maleflowers of greater than 7.0 at day 22, including an average number ofmale flowers at day 22 in the range of whole integers and parts thereof,including 7.0, 8.0, 9.0, 10.0, 11.0, 12.0, 13.0, 14.0, 15.0, 16.0, 17.0,18.0, 19.0, 20.0, and 21.0.

This present invention is directed to developing unique plants of theCitrullus species. The watermelon plant of the present inventionexpresses a substantial increase in branching resulting in a compactplant. A transferable gene or allele, designated HMBN, that conveys thischaracteristic has been isolated and incorporated into other geneticbackgrounds. The allele of the instant invention has also been expressedin different genetic backgrounds of watermelon.

EXAMPLES

The following examples are provided to further illustrate the presentinvention and are not intended to limit the invention beyond thelimitations set forth in the appended claims.

Example 1

The HMBN allele of the present invention greatly increases the number ofsecondary branches per plant. Tested standard diploid varieties averaged16 secondary branches per plant; tested dwarfs ranged from 3 to 25secondary branches with an average of 11.3 per plant. The multibranchinglines of the present invention ranged from 32 to 72 secondary branchesper plant with an average of 44.9. In the instant invention, the plantsare visibly smaller than standard diploid varieties. The average longestbranch of the present invention is 142.8 cm compared to 226.7 cm of astandard diploid variety. The six different tested dwarf lines averaged100.6 cm for the longest branch, less than both the multibranching linesof the present invention and the standard diploids. In the presentinvention, the plants also have noticeably smaller internodes than thestandard diploids but not as small as the dwarf lines.

As shown in Table 1 below, a variety containing the HMBN allele of thepresent invention, HMBN, is compared to two dwarf varieties, J86 (dw-2)and Bush Jubilee (dw-1), and to a standard diploid variety, Allsweet.

TABLE 1 Variety Bush Character HMBN J86 Jubilee Allsweet Ave. longestbranch 142.8 cm 116 cm 120.7 cm 226.7 cm Range of longest branch 101-177cm 94-136 cm 111-126 cm 195-244 cm Ave. shortest branch 55.1 cm 54.3 cm76.3 cm 124.0 cm Range of shortest branch 27-72 cm 44-71 cm 61-100 cm105-135 cm Ave. no. of primary branches 6.9 5.8 5.3 4.7 Range of no. ofprimary branches 5-10 5-7 5-6 4-5 Ave. no. of secondary 44.9 19.3 7.314.7 branches at 30 cm Range of no. of 32-65 17-23 7-8 12-17 secondarybranches at 30 cm Ave. no. of secondary 49.3 18.3 6.3 14.7 branches at90 cm Range of no. of 37-72 13-22 5-7 13-17 secondary branches at 90 cmAve. length of internodes 4.4 cm 3.4 cm 4.1 cm 7.2 cm Range of length ofinternodes 3-6 cm 2.2-4.6 cm 4-4.6 cm 5.4-9.8 cm

The HMBN allele of the present invention causes a very visible increasein the number of flowers per plant compared to both the tested dwarflines and the diploid standards. This increase in the number of flowersapplies to both male and female flowers and is constant during theflowering period.

In Table 2 below, a variety containing the HMBN allele of the presentinvention, HMBN, is compared to two dwarf varieties, J86 and BushJubilee, and to a standard diploid, Allsweet, for the number of flowersper plant over a 22 day flowering period.

TABLE 2 Average number of male/female flowers per plant for each varietyHMBN J86 Bush Jubilee Allsweet Male flowers day 1 7 3 1 3 Range of maleflowers  1-16 2-6  0-2 1-3 day 1 Female flowers day 1 1 0 0 0 Range offemale flowers 0-4 0 0 0-1 day 1 Male flowers day 8 27 12 6 5 Range ofmale flowers  4-53 8-15  3-11 3-7 day 8 Female flowers day 8 3 1 1 0Range of female flowers 0-7 0-3  1-3 0 day 8 Male flowers day 15 19 10 83 Range of male flowers  5-38 5-13 6-9 3-4 day 15 Female flowers day 152 1 2 0 Range of female flowers 0-6 0-3  1-2 0 day 15 Male flowers day22 13 7 4 1 Range of male flowers  0-21 1-16 4-5 0-1 day 22 Femaleflowers day 22 1 0 1 0 Range of female flowers 0-4 0 0-2 0 day 22

The HMBN allele of the present invention also increases the number offruit per plant compared to the tested dwarf and standard diploidvarieties. The multibranching lines of the present invention average 9.1fruit per plant whereas the dwarf lines average 1.8 fruit per plant andthe standard diploid variety averages 1.0 fruit per plant. The fruitweight of the varieties containing the HMBN allele of the presentinvention also were smaller than the standard diploids, 1.6 kg comparedto 8.98 kg.

In Table 3, a variety containing the HMBN allele of the presentinvention, HMBN, is compared to two dwarf varieties, J86 and BushJubilee, and a standard diploid variety, Allsweet, for leaf and fruitcharacteristics.

TABLE 3 Variety Leaf and fruit Bush characters HMBN J86 Jubilee AllsweetAve. leaf 8.7 8.8 9.8 11.3 width (cm) Range of leaf 6-12 7.5-9.5 11-1610-14.5 width (cm) Ave. leaf 10.0 13.0 18.3 19.7 length (cm) Range ofleaf 7-14 10.5-21.5 13-20 16-22   length (cm) Ave. fruit 9.1 2.7 1.0 1.0number Range of 7-13 1-4 1 1 fruit number Ave. fruit 0.87 3.7 5.6 8.98weight (kg) Range of fruit 0.72-1.01  2.9-4.6 4.8-6.3 7.37-11.13  weight(kg)

Example 2

The HMBN line and the two dwarf lines, J86 and Bush Jubilee, werecrossed to produce all possible F₁ combinations. All F₁s resulted innormal vine types indicating that the HMBN, dw-1 and dw-2 genes aredifferent single recessive genes.

Example 3

In Table 4, two different F₁ populations of Normal/HMBN each were selfedto produce F₂ progeny. The Normal line was HM17. The results of the F₂segregation data fit the expected 3:1 phenotypic ratio, indicating theHMBN allele is a single recessive allele.

TABLE 4 Total Number Number of Number of F₂ Population of Plants NormalPlants HMBN Plants Population #1 266 199 66 Population #2 247 184 60

Example 4

In Table 5 below, one separate F₁ population of HMBN/dw-1 was selfed toproduce F₂ progeny. The results of the F₂ segregation data fit the9:3:3:1 phenotypic ratio, indicating that the HMBN and dw-1 genes act assingle recessive genes at different loci.

TABLE 5 Number of each phenotype - Total number of progeny consisted of47 plants 27 Normal 13 dw-1 6 HMBN 2 dw-1/HMBN

Example 5

In Table 6 below, a different F₁ population of HMBN/dw-2 was selfed toproduce F₂ progeny. The results of the F₂ segregation data fit the9:3:3:1 phenotypic ratio, indicating that the HMBN and dw-2 genes act assingle recessive genes at different loci.

TABLE 6 Number of each phenotype - Total number of progeny consisted of79 plants 40 Normal 17 dw-2 16 HMBN 6 dw-2/HMBN

Example 6

In Table 7 below, the external fruit firmness of HMBN genotypes havingthe HMBN allele were compared to Sangria using penetrometer readings inpounds (taken with a Fruit Pressure Tester, model FT327 and using an 8.0mm tip). The average penetrometer reading, in pounds, for the varietycontaining the HMBN allele was 6.93 while the average for Sangria was17.27.

TABLE 7 HMBN External Fruit Firmness compared to Sangria Wt Fruit#Penetrometer (kg) 1 6.90 0.78 2 9.45 0.92 3 6.40 0.68 4 7.70 0.64 5 9.401.04 6 5.50 0.48 7 5.30 0.62 8 7.20 0.78 9 6.10 0.64 10 7.90 0.66 116.80 0.88 12 6.80 0.74 13 6.85 0.78 14 7.00 0.68 15 6.20 0.62 16 6.400.68 17 7.00 0.70 18 7.80 0.56 19 7.70 0.66 20 5.10 0.78 21 6.30 0.60 226.50 0.68 23 9.50 0.44 24 6.50 0.88 25 7.20 1.22 26 7.00 0.74 27 6.600.72 28 5.90 0.66 29 5.10 0.80 30 6.85 0.76 31 4.50 0.82 32 6.90 0.64 335.70 0.80 34 7.00 0.98 35 5.90 0.74 36 7.70 0.68 37 4.40 0.66 38 6.200.82 39 6.10 0.82 40 6.60 0.74 41 7.75 0.76 42 6.25 0.82 43 7.10 0.82 4410.70 0.76 45 5.90 0.52 46 6.40 0.74 47 7.00 0.86 48 6.75 0.84 49 6.901.08 50 6.40 0.96 51 10.00 0.84 52 6.10 0.68 53 6.40 0.86 54 5.90 0.6855 6.35 0.84 56 7.70 0.56 57 6.10 0.74 58 6.80 0.58 59 6.70 0.68 60 6.650.74 61 9.60 0.80 62 6.80 0.84 63 6.00 0.76 64 7.00 0.72 65 6.20 0.58 667.30 0.94 67 6.50 0.72 68 6.80 0.54 69 7.40 0.76 70 6.70 0.68 71 5.600.86 72 5.45 0.80 73 7.30 0.70 74 7.10 0.68 75 7.70 0.78 76 10.50 0.7277 7.30 0.76 78 7.00 0.80 79 4.90 0.62 80 6.55 0.72 81 8.50 0.84 82 6.900.70 83 7.30 0.62 84 7.30 0.70 85 5.10 0.54 86 7.00 0.54 87 5.20 0.58 887.40 0.54 89 7.90 0.50 90 6.20 0.60 91 5.90 0.62 92 7.20 0.70 93 9.100.50 94 6.45 0.62 95 7.40 0.58 96 5.90 0.60 97 8.60 0.80 98 9.40 0.64 996.30 0.64 100 6.20 0.52 101 6.00 0.85 102 8.20 0.62 103 7.10 0.48 1049.10 0.80 105 6.10 0.76 106 5.60 0.62 107 5.35 0.48 108 9.00 0.70 1098.70 0.74 110 6.10 0.78 111 7.00 0.64 112 6.65 0.58 113 7.30 0.66 1147.00 0.66 115 8.50 0.64 116 8.00 0.66 117 6.40 0.82 118 8.20 0.72 1197.20 0.46 120 5.40 0.64 121 6.60 0.72 122 6.90 0.93 123 6.30 0.70 1246.15 0.60 125 9.70 0.66 Average 6.93 0.71 Sangria 13.20 6.84 Sangria17.30 9.58 Sangria 21.30 8.68 Average 17.27 8.37

FURTHER EMBODIMENTS OF THE INVENTION

This invention also is directed to methods for producing a watermelonplant by crossing a first parent watermelon plant with a second parentwatermelon plant wherein either the first or second parent watermelonplant contains the HMBN allele of the present invention. Further, thisinvention also is directed to methods for producing an inbred watermelonline HMBN-derived watermelon plant by crossing an inbred watermelon linecontaining the HMBN allele with a second watermelon plant and growingthe progeny seed, and repeating the crossing and growing steps with theinbred watermelon line HMBN-derived plant from 1, 2, 3, 4, 5, 6 to 7times. Thus, any such methods using a watermelon line containing theHMBN allele are part of this invention: selfing, backcrosses, hybridproduction, crosses to populations, and the like. All plants producedusing a watermelon line containing the HMBN allele as a parent arewithin the scope of this invention, including plants derived from inbredwatermelon lines having HMBN.

It should be understood that the inbred could, through routinemanipulation of cytoplasmic or other factors, be produced in amale-sterile form. Such embodiments are also contemplated within thescope of the present claims.

As used herein, the term “plant” includes plant cells, plantprotoplasts, plant cell tissue cultures from which watermelon plants canbe regenerated, plant calli, plant clumps and plant cells that areintact in plants or parts of plants, such as embryos, pollen, ovules,flowers, leaves, stalks, and the like.

As it is well known in the art, tissue culture of watermelon can be usedfor the in vitro regeneration of watermelon plants. Tissues cultures ofvarious tissues of watermelon and regeneration of plants therefrom arewell known and published. By way of example, a tissue culture comprisingorgans has been used to produce regenerated plants as described inRegeneration and Micropropagation: Techniques, Systems and Media1991-1995, in Herman, E. B., ed., Recent Advances in Plant TissueCulture, Volume 3 (1995); Desamero et al., Plant Cell Tiss. Org. Cult.33:265-271 (1993); Tabei et al., Plant Tiss. Cult. Lett. 10:235 (1993).Thus, another aspect of this invention is to provide cells which, upongrowth and differentiation, produce watermelon plants having thephysiological and morphological characteristics of a watermelon linecontaining the HMBN allele.

With the advent of molecular biological techniques allowing theisolation and characterization of genes that encode specific proteinproducts, scientists in the field of plant biology developed a stronginterest in engineering the genome of plants to contain and expressforeign genes, or additional or modified versions of native, orendogenous, genes (perhaps driven by different promoters) in order toalter the traits of a plant in a specific manner. Such foreignadditional and/or modified genes are referred to herein collectively as“transgenes”. Over the last fifteen to twenty years several methods forproducing transgenic plants have been developed, and the presentinvention in particular embodiments also relates to transformed versionsof the claimed plants having the mutant allele.

Plant transformation involves the construction of an expression vectorwhich will function in plant cells. Such a vector comprises DNAcomprising a gene under control of, or operatively linked to, aregulatory element (for example, a promoter). The expression vector maycontain one or more such operably linked gene/regulatory elementcombinations. The vector(s) may be in the form of a plasmid, and can beused alone or in combination with other plasmids, to provide transformedwatermelon plants, using transformation methods as described below toincorporate transgenes into the genetic material of the watermelonplant(s).

Expression Vectors for Watermelon Transformation

Marker Genes—Expression vectors include at least one genetic marker,operably linked to a regulatory element (a promoter, for example) thatallows transformed cells containing the marker to be either recovered bynegative selection, i.e., inhibiting growth of cells that do not containthe selectable marker gene, or by positive selection, i.e., screeningfor the product encoded by the genetic marker. Many commonly usedselectable marker genes for plant transformation are well known in thetransformation arts, and include, for example, genes that code forenzymes that metabolically detoxify a selective chemical agent which maybe an antibiotic or an herbicide, or genes that encode an altered targetwhich is insensitive to the inhibitor. A few positive selection methodsare also known in the art.

One commonly used selectable marker gene for plant transformation is theneomycin phosphotransferase II (nptII) gene, isolated from transposonTn5, which, when placed under the control of plant regulatory signals,confers resistance to kanamycin. Fraley et al., Proc. Natl. Acad. Sci.U.S.A., 80:4803 (1983) Eck et al., Plant Cell Report, 14:5 299-304(1995). Another commonly used selectable marker gene is the hygromycinphosphotransferase gene which confers resistance to the antibiotichygromycin. Vanden Elzen et al., Plant Mol. Biol., 5:299 (1985).

Additional selectable marker genes of bacterial origin that conferresistance to antibiotics include gentamycin acetyl transferase,streptomycin phosphotransferase and aminoglycoside-3′-adenyltransferase, the bleomycin resistance determinant. Hayford et al., PlantPhysiol. 86:1216 (1988), Jones et al., Mol. Gen. Genet., 210:86 (1987),Svab et al., Plant Mol. Biol. 14:197 (1990), Hille et al., Plant Mol.Biol. 7:171 (1986). Other selectable marker genes confer resistance toherbicides such as glyphosate, glufosinate or broxynil. Comai et al.,Nature 317:741-744 (1985), Gordon-Kamm et al., Plant Cell 2:603-618(1990) and Stalker et al., Science 242:419-423 (1988).

Selectable marker genes for plant transformation which are not ofbacterial origin include, for example, mouse dihydrofolate reductase,plant 5-enol-pyruvyl-shikimate-3-phosphate synthase and plantacetolactate synthase. Eichholtz et al., Somatic Cell Mol. Genet 13:67(1987), Shah et al., Science 233:478 (1986), Charest et al., Plant CellRep. 8:643 (1990).

Another class of marker genes for plant transformation requiresscreening of presumptively transformed plant cells rather than directgenetic selection of transformed cells for resistance to a toxicsubstance such as an antibiotic. These genes are particularly useful toquantify or visualize the spatial pattern of expression of a gene inspecific tissues and are frequently referred to as reporter genesbecause they can be fused to a gene or gene regulatory sequence for theinvestigation of gene expression. Commonly used genes for screeningpresumptively transformed cells include beta-glucuronidase (GUS),alpha-galactosidase, luciferase and chloramphenicol acetyltransferase.Jefferson, R. A., Plant Mol. Biol. Rep. 5:387 (1987), Teeri et al., EMBOJ. 8:343 (1989), Koncz et al., Proc. Natl. Acad. Sci U.S.A. 84:131(1987), DeBlock et al., EMBO J. 3:1681 (1984), Charng et al., PlantScience Limerick. 1994, 98: 2, 175-183, Hu Wei e al., In vitro Cellularand Developmental Biology Plant 37:1 12-18 (2001), Agharbaoui et al.,Plant Cell Report 15:1/2 102-105 (1995).

In vivo methods for visualizing GUS activity that do not requiredestruction of plant tissue are available. Molecular Probes publication2908, IMAGENE GREEN, p. 1-4 (1993) and Naleway et al., J. Cell Biol.115:151a (1991). However, these in vivo methods for visualizing GUSactivity have not proven useful for recovery of transformed cellsbecause of low sensitivity, high fluorescent backgrounds and limitationsassociated with the use of luciferase genes as selectable markers.

A gene encoding Green Fluorescent Protein (GFP) has been utilized as amarker for gene expression in prokaryotic and eukaryotic cells. Chalfieet al., Science 263:802 (1994). GFP and mutants of GFP may be used asscreenable markers.

Promoters—Genes included in expression vectors must be driven by anucleotide sequence comprising a regulatory element, for example, apromoter. Several types of promoters are now well known in thetransformation arts, as are other regulatory elements that can be usedalone or in combination with promoters.

As used herein, “promoter” includes reference to a region of DNAupstream from the start of transcription and involved in recognition andbinding of RNA polymerase and other proteins to initiate transcription.A plant promoter is a promoter capable of initiating transcription inplant cells. Examples of promoters under developmental control includepromoters that preferentially initiate transcription in certain tissues,such as leaves, roots, seeds, fibers, xylem vessels, tracheids, orsclerenchyma. Such promoters are referred to as “tissue-preferred”.Promoters which initiate transcription only in certain tissue arereferred to as “tissue-specific”. A “cell type” specific promoterprimarily drives expression in certain cell types in one or more organs,for example, vascular cells in roots or leaves. An “inducible” promoteris a promoter which is under environmental control. Examples ofenvironmental conditions that may effect transcription by induciblepromoters include anaerobic conditions or the presence of light.Tissue-specific, tissue-preferred, cell type specific, and induciblepromoters constitute the class of “non-constitutive” promoters. A“constitutive” promoter is a promoter which is active under mostenvironmental conditions.

A. Inducible Promoters

An inducible promoter is operably linked to a gene for expression inwatermelon. Optionally, the inducible promoter is operably linked to anucleotide sequence encoding a signal sequence which is operably linkedto a gene for expression in watermelon. With an inducible promoter therate of transcription increases in response to an inducing agent.

Any inducible promoter can be used in the instant invention. See Ward etal., Plant Mol. Biol. 22:361-366 (1993). Exemplary inducible promotersinclude, but are not limited to, that from the ACEI system whichresponds to copper (Meft et al., PNAS 90:4567-4571 (1993)); In2 genefrom maize which responds to benzenesulfonamide herbicide safeners(Hershey et al., Mol. Gen Genetics 227:229-237 (1991) and Gatz et al.,Mol. Gen. Genetics 243:32-38 (1994)) or Tet repressor from Tn10 (Gatz etal., Mol. Gen. Genetics 227:229-237 (1991)). A particularly preferredinducible promoter is a promoter that responds to an inducing agent towhich plants do not normally respond. An exemplary inducible promoter isthe inducible promoter from a steroid hormone gene, the transcriptionalactivity of which is induced by a glucocorticosteroid hormone (Schena etal., Proc. Natl. Acad. Sci. U.S.A. 88:0421 (1991)).

B. Constitutive Promoters

A constitutive promoter is operably linked to a gene for expression inwatermelon or the constitutive promoter is operably linked to anucleotide sequence encoding a signal sequence which is operably linkedto a gene for expression in watermelon.

Many different constitutive promoters can be utilized in the instantinvention. Exemplary constitutive promoters include, but are not limitedto, the promoters from plant viruses such as the 35S promoter from CaMV(Odell et al., Nature 313:810-812. (1985), Tababeizadeh et al., PlantCell Report 19:2 197-202 (1999), Kunik et al., Acta Horticulturae 447,387-391 (1997)) and the promoters from such genes as rice actin (McElroyet al., Plant Cell 2:163-171 (1990)); ubiquitin (Christensen et al.,Plant Mol. Biol. 12:619-632 (1989) and Christensen et al., Plant Mol.Biol. 18:675-689 (1992)); pEMU (Last et al., Theor. Appl. Genet.81:581-588 (1991)); MAS (Velten et al., EMBO J. 3:2723-2730 (1984)) andmaize H3 histone (Lepetit et al., Mol. Gen. Genetics 231:276-285 (1992)and Atanassova et al., Plant Journal 2 (3): 291-300 (1992)).

The ALS promoter, Xba1/NcoI fragment, 5′ to the Brassica napus ALS3structural gene (or a nucleotide sequence similar to said Xba1/NcoIfragment), represents a particularly useful constitutive promoter. SeePCT application WO96/30530.

C. Tissue-Specific or Tissue-Preferred Promoters

A tissue-specific promoter is operably linked to a gene for expressionin watermelon. Optionally, the tissue-specific promoter is operablylinked to a nucleotide sequence encoding a signal sequence which isoperably linked to a gene for expression in watermelon. Plantstransformed with a gene of interest operably linked to a tissue-specificpromoter produce the protein product of the transgene exclusively, orpreferentially, in a specific tissue.

Any tissue-specific or tissue-preferred promoter can be utilized in theinstant invention. Exemplary tissue-specific or tissue-preferredpromoters include, but are not limited to, a root-preferred promoter,such as that from the phaseolin gene (Murai et al., Science 23:476-482(1983) and Sengupta-Gopalan et al., Proc. Natl. Acad. Sci. U.S.A.82:3320-3324 (1985)), such as the promoter rolD from Agrobacteriumrhizogenes as mentioned in Grichko et al., Plant Physiology andBiochemistry 39:1 19-25 (2001); a leaf-specific and light-inducedpromoter such as that from cab or rubisco (Simpson et al., EMBO J.4(11):2723-2729 (1985) and Timko et al., Nature 318:579-582 (1985)); ananther-specific promoter such as that from LAT52 (Twell et al., Mol.Gen. Genetics 217:240-245 (1989)); a pollen-specific promoter such asthat from Zm13 (Guerrero et al., Mol. Gen. Genetics 244:161-168 (1993))or a microspore-preferred promoter such as that from apg (Twell et al.,Sex. Plant Reprod. 6:217-224 (1993)).

Signal Sequences for Targeting Proteins to Subcellular Compartments

Transport of protein produced by transgenes to a subcellular compartmentsuch as the chloroplast, vacuole, peroxisome, glyoxysome, cell wall ormitochondrion or for secretion into the apoplast, is accomplished bymeans of operably linking the nucleotide sequence encoding a signalsequence to the 5′ and/or 3′ region of a gene encoding the protein ofinterest. Targeting sequences at the 5′ and/or 3′ end of the structuralgene may determine, during protein synthesis and processing, where theencoded protein is ultimately compartmentalized.

The presence of a signal sequence directs a polypeptide to either anintracellular organelle or subcellular compartment or for secretion tothe apoplast. Many signal sequences are known in the art. See, forexample Becker et al., Plant Mol. Biol. 20:49 (1992); Close, P. S.,Master's Thesis, Iowa State University (1993); Knox, C., et al., PlantMol. Biol. 9:3-17 (1987); Lerner et al., Plant Physiol. 91:124-129(1989); Fontes et al., Plant Cell 3:483-496 (1991); Matsuoka et al.,Proc. Natl. Acad. Sci. 88:834 (1991); Gould et al., J. Cell. Biol.108:1657 (1989); Creissen et al., Plant J. 2:129 (1991); Kalderon, etal., Cell 39:499-509 (1984); Steifel, et al., Plant Cell 2:785-793(1990).

Foreign Protein Genes and Agronomic Genes

With transgenic plants according to the present invention, a foreignprotein can be produced in commercial quantities. Thus, techniques forthe selection and propagation of transformed plants, which are wellunderstood in the art, yield a plurality of transgenic plants which areharvested in a conventional manner, and a foreign protein then can beextracted from a tissue of interest or from total biomass. Proteinextraction from plant biomass can be accomplished by known methods whichare discussed, for example, by Heney and Orr, Anal. Biochem. 114:92-6(1981).

According to a preferred embodiment, the transgenic plant provided forcommercial production of foreign protein is watermelon. In anotherpreferred embodiment, the biomass of interest is seed. For therelatively small number of transgenic plants that show higher levels ofexpression, a genetic map can be generated, primarily via conventionalRFLP, PCR and SSR analysis, which identifies the approximate chromosomallocation of the integrated DNA molecule. For exemplary methodologies inthis regard, see Glick and Thompson, Methods in Plant Molecular Biologyand Biotechnology CRC Press, Boca Raton 269:284 (1993). Map informationconcerning chromosomal location is useful for proprietary protection ofa subject transgenic plant. If unauthorized propagation is undertakenand crosses made with other germplasm, the map of the integration regioncan be compared to similar maps for suspect plants, to determine if thelatter have a common parentage with the subject plant. Map comparisonswould involve hybridizations, RFLP, PCR, SSR and sequencing, all ofwhich are conventional techniques.

Likewise, by means of the present invention, agronomic genes can beexpressed in transformed plants. More particularly, plants can begenetically engineered to express various phenotypes of agronomicinterest. Exemplary genes implicated in this regard include, but are notlimited to, those categorized below:

1. Genes that Confer Resistance to Pests or Disease and that Encode:

A. Plant disease resistance genes. Plant defenses are often activated byspecific interaction between the product of a disease resistance gene(R) in the plant and the product of a corresponding avirulence (Avr)gene in the pathogen. A plant mutant allele can be transformed withcloned resistance gene(s) to engineer plants that are resistant tospecific pathogen strains. See, for example Jones et al., Science266:789 (1994) (cloning of the tomato Cf-9 gene for resistance toCladosporium fulvum); Martin et al., Science 262:1432 (1993) (tomato Ptogene for resistance to Pseudomonas syringae pv. tomato encodes a proteinkinase); Mindrinos et al., Cell 78:1089 (1994) (Arabidopsis RSP2 genefor resistance to Pseudomonas syringae).

B. A Bacillus thuringiensis protein, a derivative thereof or a syntheticpolypeptide modeled thereon. See, for example, Geiser et al., Gene48:109 (1986), who disclose the cloning and nucleotide sequence of aBt-δ-endotoxin gene. Moreover, DNA molecules encoding δ-endotoxin genescan be purchased from American Type Culture Collection, Manassas, Va.,for example, under ATCC Accession Nos. 40098, 67136, 31995 and 31998.See also Mandaokat et al., Crop Protection. 2000, 19: 5, 307-312.

C. A lectin. See, for example, the disclosure by Van Damme et al., PlantMolec. Biol. 24:25 (1994), who disclose the nucleotide sequences ofseveral Clivia miniata mannose-binding lectin genes.

D. Genes coding for the coat proteins of the Cucumber Mosaic virus(CMV), see Tomassoli et al., Molecular Breeding. 1999, 5: 2, 121-130,which confers resistance to CMV.

E. An enzyme inhibitor, for example, a protease or proteinase inhibitoror an amylase inhibitor or a polygalacturonase inhibitor protein. See,for example, Abe et al., J. Biol. Chem. 262:16793 (1987) (nucleotidesequence of rice cysteine proteinase inhibitor), Huub et al., PlantMolec. Biol. 21:985 (1993) (nucleotide sequence of cDNA encoding tobaccoproteinase inhibitor 1), Sumitani et al., Biosci. Biotech. Biochem.57:1243 (1993) (nucleotide sequence of Streptomyces nitrosporeusα-amylase inhibitor) and Powell et al., Molecular Plant MicrobeInteraction. 2000, 13: 9 942-950 (tomatoes transformed with pear fruitpolygalacturonase inhibitor protein to inhibit fungal pathogenendopolygalacturonase).

F. An insect-specific hormone or pheromone such as an ecdysteroid orjuvenile hormone, a variant thereof, a mimetic based thereon, or anantagonist or agonist thereof. See, for example, the disclosure byHammock et al., Nature 344:458 (1990), of baculovirus expression ofcloned juvenile hormone esterase, an inactivator of juvenile hormone.

G. An insect-specific peptide or neuropeptide which, upon expression,disrupts the physiology of the affected pest. For example, see thedisclosures of Regan, J. Biol. Chem. 269:9 (1994) (expression cloningyields DNA coding for insect diuretic hormone receptor), and Pratt etal., Biochem. Biophys. Res. Comm. 163:1243 (1989) (an allostatin isidentified in Diploptera puntata). See also U.S. Pat. No. 5,266,317 toTomalski et al., who disclose genes encoding insect-specific, paralyticneurotoxins.

H. An insect-specific venom produced in nature by a snake, a wasp, etc.For example, see Pang et al., Gene 116:165 (1992), for disclosure ofheterologous expression in plants of a gene coding for a scorpioninsectotoxic peptide.

I. An enzyme responsible for a hyper-accumulation of a monoterpene, asesquiterpene, a steroid, a hydroxamic acid, a phenylpropanoidderivative or another non-protein molecule with insecticidal activity.

J. An enzyme involved in the modification, including thepost-translational modification, of a biologically active molecule; forexample, a glycolytic enzyme, a proteolytic enzyme, a lipolytic enzyme,a nuclease, a cyclase, a transaminase, an esterase, a hydrolase, aphosphatase, a kinase, a phosphorylase, a polymerase, an elastase, achitinase and a glucanase, whether natural or synthetic. See PCTapplication WO 93/02197 in the name of Scott et al., which discloses thenucleotide sequence of a callase gene. DNA molecules which containchitinase-encoding sequences can be obtained, for example, from the ATCCunder Accession Nos. 39637 and 67152. See also Kramer et al., InsectBiochem. Molec. Biol. 23:691 (1993), who teach the nucleotide sequenceof a cDNA encoding tobacco hookworm chitinase, and Kawalleck et al.,Plant Molec. Biol. 21:673 (1993), who provide the nucleotide sequence ofthe parsley ubi4-2 polyubiquitin gene.

K. A molecule that stimulates signal transduction. For example, see thedisclosure by Botella et al., Plant Molec. Biol. 24:757 (1994), ofnucleotide sequences for mung bean calmodulin cDNA clones, and Griess etal., Plant Physiol. 104:1467 (1994), who provide the nucleotide sequenceof a maize calmodulin cDNA clone.

L. A hydrophobic moment peptide. See PCT application WO95/16776(disclosure of peptide derivatives of Tachyplesin which inhibit fungalplant pathogens) and PCT application WO95/18855 (teaches syntheticantimicrobial peptides that confer disease resistance).

M. A membrane permease, a channel former or a channel blocker. Forexample, see the disclosure of Jaynes et al., Plant Sci 89:43 (1993), ofheterologous expression of a cecropin-β lytic peptide analog to rendertransgenic tobacco plants resistant to Pseudomonas solanacearum.

N. A viral-invasive protein or a complex toxin derived therefrom. Forexample, the accumulation of viral coat proteins in transformed plantcells imparts resistance to viral infection and/or disease developmenteffected by the virus from which the coat protein gene is derived, aswell as by related viruses. See Beachy et al., Ann. Rev. Phytopathol.28:451 (1990). Coat protein-mediated resistance has been conferred upontransformed plants against alfalfa mosaic virus, cucumber mosaic virus,tobacco streak virus, potato virus X, potato virus Y, tobacco etchvirus, tobacco rattle virus and tobacco mosaic virus.

O. An insect-specific antibody or an immunotoxin derived therefrom.Thus, an antibody targeted to a critical metabolic function in theinsect gut would inactivate an affected enzyme, killing the insect. Cf.Taylor et al., Abstract #497, Seventh Int'l Symposium on MolecularPlant-Microbe Interactions (Edinburgh, Scotland) (1994) (enzymaticinactivation in transgenic tobacco via production of single-chainantibody fragments).

P. A virus-specific antibody. See, for example, Tavladoraki et al.,Nature 366:469 (1993), who show that transgenic plants expressingrecombinant antibody genes are protected from virus attack.

Q. A developmental-arrestive protein produced in nature by a pathogen ora parasite. Thus, fungal endo-α-1,4-D-polygalacturonases facilitatefungal colonization and plant nutrient release by solubilizing plantcell wall homo-α-1,4-D-galacturonase. See Lamb et al., Bio/Technology10:1436 (1992). The cloning and characterization of a gene which encodesa bean endopolygalacturonase-inhibiting protein is described by Toubartet al., Plant J. 2:367 (1992).

R. A developmental-arrestive protein produced in nature by a plant. Forexample, Logemann et al., Bioi/Technology 10:305 (1992), have shown thattransgenic plants expressing the barley ribosome-inactivating gene havean increased resistance to fungal disease.

2. Genes that Confer Resistance to an Herbicide, for Example:

A. An herbicide that inhibits the growing point or meristem such as animidazolinone or a sulfonylurea. Exemplary genes in this category codefor mutant ALS and AHAS enzyme as described, for example, by Lee et al.,EMBO J. 7:1241 (1988), and Miki et al., Theor. Appl. Genet. 80:449(1990), respectively.

B. Glyphosate (resistance impaired by mutant5-enol-pyruvylshikimate-3-phosphate synthase (EPSP) and aroA genes,respectively) and other phosphono compounds such as glufosinate(phosphinothricin acetyl transferase (PAT) and Streptomyceshygroscopicus PAT, bar, genes), and pyridinoxy or phenoxy propionicacids and cyclohexones (ACCase inhibitor-encoding genes). See, forexample, U.S. Pat. No. 4,940,835 to Shah, et al., which discloses thenucleotide sequence of a form of EPSP which can confer glyphosateresistance. A DNA molecule encoding a mutant aroA gene can be obtainedunder ATCC accession number 39256, and the nucleotide sequence of themutant gene is disclosed in U.S. Pat. No. 4,769,061 to Comai. Europeanpatent application No. 0 333 033 to Kumada et al., and U.S. Pat. No.4,975,374 to Goodman et al., disclose nucleotide sequences of glutaminesynthetase genes which confer resistance to herbicides such asL-phosphinothricin. The nucleotide sequence of a PAT gene is provided inEuropean application No. 0 242 246 to Leemans et al. DeGreef et al.,Bio/Technology 7:61 (1989), describe the production of transgenic plantsthat express chimeric bar genes coding for PAT activity. Exemplary ofgenes conferring resistance to phenoxy propionic acids and cyclohexones,such as sethoxydim and haloxyfop are the Acc1-S1, Acc1-S2 and Acc1-S3genes described by Marshall et al., Theor. Appl. Genet. 83:435 (1992).

C. An herbicide that inhibits photosynthesis, such as a triazine (psbAand gs+ genes) or a benzonitrile (nitrilase gene). Przibilla et al.,Plant Cell 3:169 (1991), describe the transformation of Chlamydomonaswith plasmids encoding mutant psbA genes. Nucleotide sequences fornitrilase genes are disclosed in U.S. Pat. No. 4,810,648 to Stalker, andDNA molecules containing these genes are available under ATCC AccessionNos. 53435, 67441, and 67442. Cloning and expression of DNA coding for aglutathione S-transferase is described by Hayes et al., Biochem. J.285:173 (1992).

3. Genes that Confer or Contribute to a Value-Added Trait. Such as:

A. Increased flooding tolerance, for example by transforming a plantwith a bacterial enzyme ACC deaminase. See Grichko et al., PlantPhysiology and Biochemistry. 2001. 39: 1, 19-25.

B. Improved juice and pulp viscosity, by transforming the plant with anantisense gene of polygalacturonase. For example, see Porretta et al.,Food Chemistry. 62:283-290 (1998) or Errington et al., Journal of theScience of Food and Agriculture, 76:515-519 (1998).

C. Reduced polyethylene production in order to better control theripening of the fruit by transforming the plant with anS-adenosylmethionine hydrolase. See Good et al., Plant MolecularBiology. 1994, 26: 3, 781-790.

D. Obtaining male sterile plants, especially useful in hybrid watermelonproduction, by introduction of a gene encoding a tobacco PR Glucanase asdescribed in WO9738116.

Methods for Watermelon Transformation

Numerous methods for plant transformation have been developed includingbiological and physical plant transformation protocols. See, forexample, Miki et al., “Procedures for Introducing Foreign DNA intoPlants” in Methods in Plant Molecular Biology and Biotechnology, GlickB. R. and Thompson, J. E. Eds. (CRC Press, Inc., Boca Raton, 1993) pages67-88. In addition, expression vectors and in vitro culture methods forplant cell or tissue transformation and regeneration of plants areavailable. See, for example, Gruber et al., “Vectors for PlantTransformation” in Methods in Plant Molecular Biology and Biotechnology,Glick B. R. and Thompson, J. E. Eds. (CRC Press, Inc., Boca Raton, 1993)pages 89-119.

A. Agrobacterium-Mediated Transformation

One method for introducing an expression vector into plants is based onthe natural transformation system of Agrobacterium. See, for example,Frary et al., Plant Cell Report. 1996, 16: 3/4, 235-240, Roehel et al.,Plant Cell Report. 1993, 12: 11, 644-647, Hu-Wei et al., In VitroCellular and Developmental Biology Plant 2001 37: 1, 12-18. A.tumefaciens and A. rhizogenes are plant pathogenic soil bacteria whichgenetically transform plant cells. The Ti and Ri plasmids of A.tumefaciens and A. rhizogenes, respectively, carry genes responsible forgenetic transformation of the plant. See, for example, Kado, C. I.,Crit. Rev. Plant Sci. 10:1 (1991). Descriptions of Agrobacterium vectorsystems and methods for Agrobacterium-mediated gene transfer areprovided by Gruber et al., supra, Miki et al., supra, and Moloney etal., Plant Cell Reports 8:238 (1989). See also, U.S. Pat. No. 6,198,022issued Mar. 6, 2001.

B. Direct Gene Transfer

Despite the fact the host range for Agrobacterium-mediatedtransformation is broad, some major cereal crop and vegetable speciesand gymnosperms have generally been recalcitrant to this mode of genetransfer, even though some success has recently been achieved in riceand corn. Hiei et al., The Plant Journal 6:271-282 (1994) and U.S. Pat.No. 5,591,616 issued Jan. 7, 1997. Several methods of planttransformation collectively referred to as direct gene transfer havebeen developed as an alternative to Agrobacterium-mediatedtransformation.

A generally applicable method of plant transformation ismicroprojectile-mediated transformation wherein DNA is carried on thesurface of microprojectiles measuring 1 to 4 μm. The expression vectoris introduced into plant tissues with a biolistic device thataccelerates the microprojectiles to speeds of 300 to 600 m/s which issufficient to penetrate plant cell walls and membranes. Sanford et al.,Part. Sci. Technol. 5:27 (1987), Sanford, J. C., Trends Biotech. 6:299(1988), Klein et al., Bio/Technology 6:559-563 (1988), Sanford, J. C.,Physiol Plant 7:206 (1990), Klein et al., Biotechnology 10:268 (1992),Baum et al., Plant Journal. 1997, 12: 2, 463-469, Eck et al., Plant CellReport. 1995, 14: 5, 299-304, Manzara et al., Plant Molecular BiologyReporter 123: 221-226 (1994).

Another method for physical delivery of DNA to plants is sonication oftarget cells. Zhang et al., Bio/Technology 9:996 (1991). Alternatively,liposome and spheroplast fusion have been used to introduce expressionvectors into plants. Deshayes et al., EMBO J., 4:2731 (1985), Christouet al., Proc Natl. Acad. Sci. U.S.A. 84:3962 (1987). Direct uptake ofDNA into protoplasts using CaCl₂ precipitation, polyvinyl alcohol orpoly-L-ornithine has also been reported. Hain et al., Mol. Gen. Genet199:161 (1985) and Draper et al., Plant Cell Physiol. 23:451 (1982).Electroporation of protoplasts and whole cells and tissues has also beendescribed. Donn et al., In Abstracts of VIIth International Congress onPlant Cell and Tissue Culture IAPTC, A2-38, p 53 (1990), D'Halluin etal., Plant Cell 4:1495-1505 (1992) and Spencer et al., Plant Mol. Biol.24:51-61 (1994). A transfer of chromosomes has been reported from atransformed donor line of potato to a recipient line of tomato throughmicroprotoplast PEG induced fusion. See Ramalu et al., Theorical andApplied Genetics 92:316-325 (1996).

Following transformation of watermelon target tissues, expression of theabove-described selectable marker genes allows for preferentialselection of transformed cells, tissues and/or plants, usingregeneration and selection methods now well known in the art.

The foregoing methods for transformation would typically be used forproducing a transgenic plant. The transgenic plant could then be crossedwith another (non-transformed or transformed) plant in order to producea new transgenic plant. Alternatively, a genetic trait which has beenengineered into a particular watermelon line using the foregoingtransformation techniques could be moved into another line usingtraditional backcrossing techniques that are well known in the plantbreeding arts. For example, a backcrossing approach could be used tomove an engineered trait from a public, non-elite variety into an elitevariety, or from a variety containing a foreign gene in its genome intoa line which does not contain that gene. As used herein, “crossing” canrefer to a simple X by Y cross, or the process of backcrossing,depending on the context.

When the term inbred watermelon plant is used in the context of thepresent invention, this also includes any single gene conversions ofthat inbred. The term single gene converted plant as used herein refersto those watermelon plants which are developed by a plant breedingtechnique called backcrossing wherein essentially all of the desiredmorphological and physiological characteristics of an inbred arerecovered in addition to the single gene transferred into the inbred viathe backcrossing technique. Backcrossing methods can be used with thepresent invention to improve or introduce a characteristic into theinbred. The term backcrossing as used herein refers to the repeatedcrossing of a hybrid progeny back to one of the parental watermelonplants for that inbred. The parental watermelon plant which contributesthe gene for the desired characteristic is termed the nonrecurrent ordonor parent. This terminology refers to the fact that the nonrecurrentparent is used one time in the backcross protocol and therefore does notrecur. The parental watermelon plant to which the gene or genes from thenonrecurrent parent are transferred is known as the recurrent parent asit is used for several rounds in the backcrossing protocol (Poehlman &Sleper, 1994; Fehr, 1987). In a typical backcross protocol, the originalinbred of interest (recurrent parent) is crossed to a second inbred(nonrecurrent parent) that carries the single gene of interest to betransferred. The resulting progeny from this cross are then crossedagain to the recurrent parent and the process is repeated until awatermelon plant is obtained wherein essentially all of the desiredmorphological and physiological characteristics of the recurrent parentare recovered in the converted plant, in addition to the singletransferred gene from the nonrecurrent parent.

The selection of a suitable recurrent parent is an important step for asuccessful backcrossing procedure. The goal of a backcross protocol isto alter or substitute a single trait or characteristic in the originalinbred. To accomplish this, a single gene of the recurrent inbred ismodified or substituted with the desired gene from the nonrecurrentparent, while retaining essentially all of the rest of the desiredgenetic, and therefore the desired physiological and morphological,constitution of the original inbred. The choice of the particularnonrecurrent parent will depend on the purpose of the backcross; one ofthe major purposes is to add some commercially desirable and/oragronomically important trait to the plant. The exact backcrossingprotocol will depend on the characteristic or trait being altered todetermine an appropriate testing protocol. Although backcrossing methodsare simplified when the characteristic being transferred is a dominantallele, a recessive allele may also be transferred. In this instance itmay be necessary to introduce a test of the progeny to determine if thedesired characteristic has been successfully transferred.

Many single gene traits have been identified that are not regularlyselected for in the development of a new inbred but that can be improvedby backcrossing techniques. Single gene traits may or may not betransgenic; examples of these traits include, but are not limited to,male sterility, such as the PR glucanase gene, herbicide resistance,such as pat or bar genes, resistance for bacterial, fungal (such as Igenes used for resistance to Fusarium oxysporum), or viral disease (suchas genes TM1 and TM2 used for TMV resistance), insect resistance such asCry1Ac or Mi genes, male fertility, enhanced nutritional quality,enhanced sugar content, enhanced conservation and delayed ripening suchas in using nor or rin genes, yield stability and yield enhancement.These genes are generally inherited through the nucleus. Some otherknown male sterility genes are inherited cytoplasmically, but still actas single gene traits. Several of these single gene traits are describedin U.S. Pat. Nos. 5,777,196; 5,948,957 and 5,969,212, the disclosures ofwhich are specifically hereby incorporated by reference.

DEPOSIT INFORMATION

A deposit of the Harris Moran Seed Company proprietary watermelon seedscontaining the HMBN mutant allele disclosed above and recited in theappended claims has been made with the American Type Culture Collection(ATCC), 10801 University Boulevard, Manassas, Va. 20110. The date ofdeposit was Nov. 12, 2004. The deposit of 2,500 seeds was taken from thesame deposit maintained by Harris Moran Seed Company since prior to thefiling date of this application. All restrictions upon the deposit willbe removed upon granting of a patent, and the deposit is intended tomeet all of the requirements of 37 C.F.R. §§1.801-1.809. The ATCCaccession number is PTA-6300. The deposit will be maintained in thedepository for a period of 30 years, or 5 years after the last request,or for the effective life of the patent, whichever is longer, and willbe replaced as necessary during that period.

Although the foregoing invention has been described in some detail byway of illustration and example for purposes of clarity andunderstanding. However, it will be obvious that certain changes andmodifications such as single gene modifications and somaclonal variants,variant individuals selected from large populations of the plants andthe like may be practiced within the scope of the invention, as limitedonly by the scope of the appended claims.

1. A triploid watermelon plant containing an allele designated HMBN,wherein a representative sample of seed containing said HMBN allele isdeposited under ATCC Accession No. PTA-6300.